A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376901



Internal ID22434771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92929294..92929373hg38UCSC Ensembl
chr14:93395639..93395718hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928539
Supporting Variants
Samples
Known GenesCHGA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376901
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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